ClinVar Miner

List of variants in gene SLC2A1 reported as benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
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Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP
NM_006516.2(SLC2A1):c.-390delA rs28365848
NM_006516.2(SLC2A1):c.-490G>C rs3754226
NM_006516.3(SLC2A1):c.*1213G>T rs55728431
NM_006516.3(SLC2A1):c.*1587A>G rs140560514
NM_006516.3(SLC2A1):c.*1588G>A rs189700252
NM_006516.3(SLC2A1):c.*22G>A rs2229683
NM_006516.3(SLC2A1):c.*346G>A rs190760291
NM_006516.3(SLC2A1):c.*462G>C rs4658
NM_006516.3(SLC2A1):c.*571C>T rs6413524
NM_006516.3(SLC2A1):c.*60C>T rs2229684
NM_006516.3(SLC2A1):c.*626G>A rs6413525
NM_006516.3(SLC2A1):c.*971G>A rs185891628
NM_006516.3(SLC2A1):c.-190G>C rs114514007
NM_006516.3(SLC2A1):c.-197A>C rs11537640
NM_006516.3(SLC2A1):c.-26G>C rs375001117
NM_006516.3(SLC2A1):c.1011C>T (p.His337=) rs2229681
NM_006516.3(SLC2A1):c.1034C>T (p.Ala345Val) rs769943554
NM_006516.3(SLC2A1):c.1065A>G (p.Leu355=) rs2228490
NM_006516.3(SLC2A1):c.1170C>T (p.Ile390=) rs2236574
NM_006516.3(SLC2A1):c.1278+9C>G rs550156548
NM_006516.3(SLC2A1):c.1372C>A (p.Arg458=) rs13306758
NM_006516.3(SLC2A1):c.138G>C (p.Gln46His) rs149998596
NM_006516.3(SLC2A1):c.1437C>T (p.Pro479=) rs146879902
NM_006516.3(SLC2A1):c.274C>A (p.Arg92=) rs202060209
NM_006516.3(SLC2A1):c.27G>A (p.Thr9=) rs34025424
NM_006516.3(SLC2A1):c.312C>G (p.Phe104Leu) rs76672402
NM_006516.3(SLC2A1):c.399C>T (p.Cys133=) rs11537641
NM_006516.3(SLC2A1):c.417C>T (p.Phe139=) rs144538918
NM_006516.3(SLC2A1):c.45C>T (p.Ala15=) rs1385129
NM_006516.3(SLC2A1):c.588G>A (p.Pro196=) rs2229682
NM_006516.3(SLC2A1):c.653G>A (p.Arg218His) rs374080633
NM_006516.3(SLC2A1):c.657C>T (p.Asn219=) rs534113895
NM_006516.3(SLC2A1):c.679+7G>C rs13306757
NM_006516.3(SLC2A1):c.679+7G>T rs13306757
NM_006516.3(SLC2A1):c.895G>A (p.Glu299Lys) rs148518827
NM_006516.3(SLC2A1):c.906G>T (p.Gly302=) rs55693364
NM_006516.3(SLC2A1):c.966C>T (p.Val322=) rs2229680
NM_006516.3(SLC2A1):c.987G>A (p.Glu329=) rs201989024
NM_006516.4(SLC2A1):c.*285C>T
NM_006516.4(SLC2A1):c.*463T>C
NM_006516.4(SLC2A1):c.798C>T (p.Pro266=)

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